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4-nitro-N-(2-(pyridine-2-yl)phenyl)benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1220100-53-7

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1220100-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1220100-53-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,0,1,0 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1220100-53:
(9*1)+(8*2)+(7*2)+(6*0)+(5*1)+(4*0)+(3*0)+(2*5)+(1*3)=57
57 % 10 = 7
So 1220100-53-7 is a valid CAS Registry Number.

1220100-53-7Downstream Products

1220100-53-7Relevant academic research and scientific papers

Dibenzothiophenesulfilimines: A Convenient Approach to Intermolecular Rhodium-Catalysed C?H Amidation

Antoni, Patrick W.,Mackenroth, Alexandra V.,Mulks, Florian F.,Rudolph, Matthias,Helmchen, Günter,Hashmi, A. Stephen K.

supporting information, p. 8235 - 8238 (2020/06/17)

A sulfilimine-based Group 9 transition-metal-catalysed C?H amidation procedure is reported. Dibenzothiophene-based sulfilimines were shown to constitute a class of novel amidation reagents which enable the transfer of a wide range of N-sulfonyl and N-acyl

Chelation-Assisted Rhodium-Catalyzed Direct Amidation with Amidobenziodoxolones: C(sp2)-H, C(sp3)-H, and Late-Stage Functionalizations

Hu, Xu-Hong,Yang, Xiao-Fei,Loh, Teck-Peng

, p. 5930 - 5934 (2016/09/09)

Air-stable and convenient amidobenziodoxolones as an amidating reagent were disclosed to enable direct amidation on a wide range of C(sp2)-H bonds of (hetero)arenes and alkenes, as well as unactivated C(sp3)-H bonds under RhIII catalysis. The approach to access 49 examples of structurally diverse amides is featured by mild conditions, complete chemoselectivity and regioselectivity, broad substrate scope (not limited to strongly heterocyclic coordinating groups), and tolerance of valuable functional substituents, such as unprotected amine and hydroxyl groups. The synthetic applicability of this protocol is also demonstrated by late-stage functionalization of biologically important scaffolds.

Rhodium(III)-catalyzed intermolecular N-chelator-directed aromatic C-H amidation with amides

Zhao, Huaiqing,Shang, Yaping,Su, Weiping

supporting information, p. 5106 - 5109 (2013/10/22)

Rh(III)-catalyzed intermolecular direct aromatic C-H bond amidation with amides has been accomplished under mild reaction conditions. This protocol is applicable to a broad range of N-chelator-containing arenes amidated with aromatic and aliphatic sulfonamides. A possible mechanism is proposed according to the experimental results.

Copper-catalyzed amidation of 2-phenylpyridine with oxygen as the terminal oxidant

John, Alex,Nicholas, Kenneth M.

experimental part, p. 4158 - 4162 (2011/07/30)

The Cu(OAc)2-catalyzed, O2-mediated amidation of 2-phenylpyridine via C-H bond activation is reported. A variety of nitrogen reagents including sulfonamides, carboxamides, and anilines participate in the reaction in moderate to good

Mechanism of C-F reductive elimination from palladium(IV) fluorides

Furuya, Takeru,Benitez, Diego,Tkatchouk, Ekaterina,Strom, Alexandra E.,Tang, Pingping,Goddard III, William A.,Ritter, Tobias

supporting information; experimental part, p. 3793 - 3807 (2010/05/15)

The first systematic mechanism study of C-F reductive elimination from a transition metal complex is described. C-F bond formation from three different Pd(IV) fluoride complexes was mechanistically evaluated. The experimental data suggest that reductive elimination occurs from cationic Pd(IV) fluoride complexes via a dissociative mechanism. The ancillary pyridyl-sulfonamide ligand plays a crucial role for C-F reductive elimination, likely due to a K 3 coordination mode, in which an oxygen atom of the sulfonyl group coordinates to Pd. The pyridyl-sulfonamide can support Pd(IV) and has the appropriate geometry and electronic structure to induce reductive elimination.

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